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[Cancer Research 66, 2700-2707, March 1, 2006]
© 2006 American Association for Cancer Research


Cell, Tumor, and Stem Cell Biology

p44 Mitogen-Activated Protein Kinase (Extracellular Signal-Regulated Kinase 1)–Dependent Signaling Contributes to Epithelial Skin Carcinogenesis

Christine Bourcier1, Arnaud Jacquel2, Jochen Hess5, Isabelle Peyrottes4, Peter Angel5, Paul Hofman3, Patrick Auberger2, Jacques Pouysségur1 and Gilles Pagès1

1 Institute of Signaling, Developmental Biology and Cancer Research, UMR Centre National de la Recherche Scientifique; 2 Unité Institut National de la Sante et de la Recherche Medicale, Equipe labellisée Ligue Nationale contre le Cancer; 3 Equipe Institut National de la Sante et de la Recherche Medicale and Laboratory of Clinical and Experimental Pathology, Faculté de Médecine, University of Nice-Sophia Antipolis; 4 Service Anatomo Pathologie Centre Antoine Lacassagne, Nice, France; and 5 Division of Signal Transduction and Growth Control, Deutsches Krebsforschungszentrum, Heidelberg, Germany

Requests for reprints: Gilles Pagès, Institute of Signaling, Developmental Biology and Cancer Research UMR Centre National de la Recherche Scientifique 6543, University of Nice-Sophia Antipolis, 33 Avenue de Valombrose, Nice, France 06189. Phone: 33-492-03-1237; Fax: 33-492-03-1235; E-mail: gpages{at}unice.fr.

Extracellular signal-regulated kinases (ERK) regulate cellular functions in response to a variety of external signals. However, the specific functions of individual ERK isoforms are largely unknown. Hence, we have investigated the specific function of ERK1 in skin homeostasis and tumorigenesis in ERK1 knockout mice. They spontaneously develop cutaneous lesions and hyperkeratosis with epidermis thickness. Skin hyperproliferation and inflammation induced by application of 12-O-tetradecanoylphorbol-13-acetate (TPA) is strongly reduced in mutant mice. ERK1–/– mice are resistant to development of skin papillomas induced by 7,12-dimethylbenz(a)anthracene (DMBA) and promoted by TPA. Tumor appearance was delayed, their formation was less frequent, and their number and size were reduced. Keratinocytes obtained from knockout mice showed reduced growth and resistance to apoptotic signals, accompanied by an impaired expression of genes implicated in growth control and invasiveness. These results highlight the importance of ERK1 in skin homeostasis and in the process of skin tumor development. (Cancer Res 2006; 66(5): 2700-7)




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